Project Delivery Associate - OptymEdge

Project Delivery Associate - OptymEdge

Location: CA Remote & US Remote

Primary Purpose 

The Project Delivery Associate (PDA) supports the successful delivery of clinical studies within a technology-enabled clinical research environment. Working within defined digital workflows and under close guidance from senior team members, the PDA executes assigned activities that support data accuracy, documentation completeness, and timely delivery. The PDA is clinical site-facing and operational in nature, focused on learning core certification processes, understanding regulated workflows, and developing foundational delivery skills. The PDA contributes to team efficiency through consistent execution, attention to detail, and effective use of systems, forming the baseline for progression into more complex and independent delivery roles.

• Supports project-specific certification activities under the direction of the Project Delivery Manager (PDM) following established digital workflows.
• Performs certification data review, validation and maintenance within electronic systems, ensuring accuracy, completeness and traceability.
• Assists in tracking project deadlines, deliverables and milestones for assigned workstreams using electronic tracking tools and templates
• Maintains study documentation within electronic systems, ensuring audit readiness and adherence to
  documentation standards.
• Performs basic quality checks by identifying inconsistencies, missing data or deviations from defined
  workflows and escalating appropriately.
• Supports coordination of conference calls, virtual meetings, and routine communications.
• Formats, tracks, and distributes technical and non-technical reports using standardized templates and tools.
• Supports the PDM in preparation of study start-up documentation and management of training requirements.
• Escalates issues, questions, or risks to the PDM or senior team members in a timely manner.
• Develops working knowledge of internal platforms and digital tools used across certification, data capture, and imaging workflows.
• Participates in team meetings and training sessions to build understanding of systems, processes and clinical trial delivery

• 2 years of relevant experience in an administrative, operational, clinical, or technology-supported environment.
• Internship, placement, or academic experience in clinical research, healthcare, life sciences, or technology-enabled operations may be considered.
• Basic proficiency with Microsoft Office applications, particularly MS Word; exposure to databases or document management systems preferred.
• Strong organizational and time-management skills, with the ability to follow defined, technology-enabled processes.
• High attention to detail and ability to manage multiple tasks with guidance and oversight from more senior team members.
• Clear written and verbal communication skills
• Interest in clinical trials, healthcare, or life sciences; ophthalmology experience preferred but not required.
• Willingness and ability to learn new systems, tools, and digital workflows in a regulated
  environment.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our  Emmes Cares  community engagement program.   We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, political affiliation, sexual orientation, gender identity, marital status, disability, protected veteran status, genetic information, age, or other legally protected characteristics.

#LI-Remote